CN113292964B - Carbon-based composite material based on popcorn as well as preparation method and application of carbon-based composite material - Google Patents

Carbon-based composite material based on popcorn as well as preparation method and application of carbon-based composite material Download PDF

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CN113292964B
CN113292964B CN202110529589.4A CN202110529589A CN113292964B CN 113292964 B CN113292964 B CN 113292964B CN 202110529589 A CN202110529589 A CN 202110529589A CN 113292964 B CN113292964 B CN 113292964B
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CN113292964A (en
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陆伟
董妍嫣
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Tongji University
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    • C01B32/05—Preparation or purification of carbon not covered by groups C01B32/15, C01B32/20, C01B32/25, C01B32/30
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    • C01G53/11—Sulfides
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    • H05K9/0073—Shielding materials
    • H05K9/0081—Electromagnetic shielding materials, e.g. EMI, RFI shielding
    • H05K9/0088—Electromagnetic shielding materials, e.g. EMI, RFI shielding comprising a plurality of shielding layers; combining different shielding material structure
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    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Abstract

The invention belongs to the field of functional materials, and particularly relates to a carbon-based composite material based on popcorn, and a preparation method and application thereof. The invention provides a carbon-based composite material based on popcorn, which is characterized in that the surface of a carbon base is covered with NiS2/SnS2Nanosheets; the carbon base is porous, and the average pore diameter is 50-200 mu m; the material consists of carbon, nickel sulfide and tin sulfide, wherein the molar ratio of the carbon to the nickel to the tin to the sulfur is (10-30): (0.5-2.2): 1: (1-6). The invention constructs coherent NiS on porous carbon base derived from popcorn2/SnS2Heterostructure nanoplatelets, first treated with NiS2/SnS2The heterostructure nanosheet is used as an absorbing material in the field of electromagnetic waves, and provides a thought for further research and application in the field of electromagnetic wave absorption.

Description

Carbon-based composite material based on popcorn as well as preparation method and application thereof
Technical Field
The invention belongs to the field of functional materials, and particularly relates to a carbon-based composite material based on popcorn, and a preparation method and application thereof.
Background
In recent years, with rapid development and wide application of wireless communication and electronic devices, electromagnetic wave (EMW) pollution is becoming more serious, which not only interferes with the operation of electronic devices, but also threatens human health and information security. Therefore, in recent years, researchers in academia have been increasingly interested in the research of electromagnetic wave absorbing materials. As is well known, electromagnetic wave absorbing materials can convert incident electromagnetic wave energy into heat energy or other forms of energy for consumption.
Generally, electromagnetic wave absorbing materials can be classified into dielectric loss materials and magnetic loss materials. On this basis, more and more electromagnetic wave absorbing materials have been successfully developed. From traditional materials such as ferrites, metal oxides, graphene and carbon nanotubes to emerging materials such as metal organic frameworks and MXene (M)n+1XnTx) Materials, which have been studied in order to satisfy the requirements of strong absorption, wide Effective Absorption Bandwidth (EAB), thin thickness and light weight of an electromagnetic wave absorber. Among them, carbonaceous materials have been an important branch of electromagnetic wave absorbing materials due to their low density, high electrical conductivity and chemical stability. Inspired by nature, biomass carbon materials have irreplaceable advantages in a series of carbonaceous materialsThe method is distinguished from other methods. First, biomass is widely distributed and abundant, including plant, animal, microbial and crop wastes. Therefore, it is a low-cost, accessible, rich and renewable natural resource; second, organisms evolve in nature over a long period of time and have a variety of unique structures, such as porous structures and channel structures. Simple pyrolytic charring processes can also inherit these primary structures. Importantly, the porous channels contribute to the dissipation of electromagnetic waves, mainly in multiple reflections and scattering, improved impedance matching, and enhanced interface polarization. In conclusion, the biomass-based carbon material not only ensures the advantages of the traditional carbon material, but also has a simpler and more economical preparation method, and accords with the composite environmental protection and sustainable concept, and in recent years, the biomass-based carbon material has become a potential candidate material for an electromagnetic wave absorbent.
However, the high conductivity of the pure carbon material is a fatal defect to further improve the wave absorption performance because it causes poor impedance matching conditions. One effective strategy is to integrate carbon materials with other components, on the one hand, to obtain a good impedance match, allowing more electromagnetic waves (EMW) to enter the absorber, and on the other hand, to give it excellent electromagnetic dissipation capabilities due to the synergistic effect and unique structural advantages of the dual dielectric materials. Tin disulfide (SnS)2) Is a typical layered metal sulfide semiconductor and is widely applied to advanced functional materials, but SnS2Poor conductivity per se, which is not favorable for improving wave absorption performance to some extent, and nickel sulfide (NiS)2) Is a typical dielectric loss material.
Disclosure of Invention
In view of the above-mentioned drawbacks of the prior art, it is an object of the present invention to provide a carbon-based composite based on popcorn, a method for preparing the same and use thereof, which solve the problems of the prior art.
To achieve the above objects and other related objects, the present invention is achieved by the following technical solutions.
One of the objects of the present invention is to provide a popcorn-based carbon-based composite material having a carbon-based surface covered with NiS2/SnS2Nanosheets; the carbon base is porous, and the average pore diameter is 50-200 mu m; the material consists of carbon, nickel sulfide and tin sulfide, wherein the molar ratio of the carbon to the nickel to the tin to the sulfur is (10-30): (0.5-2.2): 1: (1-6).
The second purpose of the present invention is to provide a method for preparing the popcorn-based carbon-based composite material, comprising the following steps: and carrying out hydrothermal reaction on the mixture of the nickel source, the tin source and the sulfur source and the carbonized popcorn to obtain the carbon-based composite material based on the popcorn.
The popcorn of the present application is popcorn from corn produced by conventional processes.
Preferably, the carbonized popcorn has a specific surface area of 2m2/g～30m2The pore diameter is 30-180 mu m.
Preferably, the preparation method of the carbonized popcorn is as follows:
and calcining the popcorn at 500-900 ℃ under a protective atmosphere to obtain the carbonized popcorn.
The calcination temperature in the invention cannot be too low or too high, and too low can cause the popcorn not to be completely carbonized and have fewer holes, and too high can cause the carbonized popcorn to have evenly distributed holes and increased macropores. The carbonized popcorn obtained by calcining at 500-900 ℃ in the invention is porous, the holes are distributed more uniformly, and the average aperture is 30-180 μm.
More preferably, the temperature rise rate of the calcination is 2 ℃/min to 10 ℃/min.
Further preferably, the temperature increase rate of the calcination is 2 ℃/min to 6 ℃/min.
More preferably, the calcination time is 80min to 200 min.
Further preferably, the calcination time is 100min to 150 min.
More preferably, the protective atmosphere is selected from one or more of nitrogen and argon.
Further preferably, the protective atmosphere is argon.
More preferably, the method further comprises the steps of washing and drying the popcorn before calcining.
Further preferably, the washing is performed by washing with water or/and absolute ethanol. Specifically, the popcorn is respectively placed in water and ethanol for ultrasonic cleaning for 3 times, and each time, the popcorn is cleaned for 5min to 20 min.
Further preferably, the drying is carried out for 20 to 30 hours at a temperature of between 40 and 80 ℃.
Preferably, the mixture is obtained by dissolving a nickel source, a sulfur source and a sulfur source in ethanol.
Preferably, the nickel source is nickel chloride. More preferably, the nickel source is nickel chloride hexahydrate.
Preferably, the tin source is tin chloride. More preferably, the tin source is tin tetrachloride pentahydrate.
Preferably, the sulfur source is thioacetamide.
More preferably, the mass ratio of the tin chloride, the nickel chloride, the thioacetamide and the ethanol is 1: (0.2-1.0): (0.2-1.6): (50-140).
Further preferably, the mass ratio of the tin chloride, the nickel chloride, the thioacetamide and the ethanol is 1: (0.2-0.5): (1.0-1.6): (50-80).
Preferably, the mass ratio of the carbonized popcorn to the tin source is 1 (2-10).
More preferably, the mass ratio of the carbonized popcorn to the tin source is 1 (3-6).
Preferably, the hydrothermal reaction is carried out for 4 to 16 hours at 100 to 200 ℃.
More preferably, the hydrothermal reaction is carried out for 6 to 10 hours at 150 to 180 ℃.
Preferably, the mixture of the nickel source, the tin source and the sulfur source and the carbonized popcorn are stirred for 4 to 12 hours and then are subjected to hydrothermal reaction.
More preferably, the hydrothermal reaction is carried out in a microwave environment.
Preferably, the hydrothermal reaction further comprises washing and drying.
More preferably, the washing is 3 times filtered and washed with water and ethanol, respectively.
More preferably, the drying temperature is 40-100 ℃.
More preferably, the drying time is 10 h-40 h.
The invention also aims to provide the application of the carbon-based composite material based on the popcorn as a wave-absorbing material in the field of electromagnetic waves.
The method comprises the steps of firstly obtaining a three-dimensional macroporous material with volume and specific surface area increased by dozens of times through a puffing process, and then obtaining a three-dimensional porous carbon base through carbonization, wherein the three-dimensional porous carbon base has the characteristic of large pores; then, through the hydrothermal reaction of the carbonized popcorn with a nickel source, a sulfur source and a sulfur source, coherent NiS is constructed on the porous carbon base2/SnS2Heterostructured nanosheets, resulting in a popcorn-based carbon-based composite. The popcorn-based carbon-based composite of the present application is a high conductivity NiS2And low conductivity SnS2Combine to form heterogeneous composite materials with different band gaps, and have excellent electromagnetic wave absorption performance due to the synergistic effect of multiple loss types, and the maximum Reflection Loss (RL) is less than 1.57mm when the thickness of the composite material ismax) 52.97dB, and the Effective Absorption Bandwidth (EAB) is 4.9 GHz.
Compared with the prior art, the invention has the following beneficial effects:
1) the invention takes the popcorn with rich source and low price as the raw material, and provides inspiration for the development of simple, environment-friendly, low-cost and feasible biomass source as the electromagnetic wave absorbing material.
2) The invention constructs coherent NiS on porous carbon base derived from popcorn2/SnS2Heterostructure nanoplate, first formed with NiS2/SnS2The heterostructure nanosheet is suitable for being used as an electromagnetic wave absorbing material in the field of electromagnetic waves, and provides a thought for further research and application in the field of electromagnetic wave absorption.
Drawings
Figure 1 shows XRD patterns of example 1, example 2, example 3, example 4 and comparative examples.
Fig. 2 shows SEM images and TEM images of examples 1, 2, 3, and 4.
Wherein the reference numerals in fig. 2 are as follows: a-SEM picture of example 3, b-SEM picture of example 3, c-TEM picture of example 3, d-SEM picture of example 1, e-SEM picture of example 2, f-SEM picture of example 4, j-TEM picture of example 3.
Fig. 3 is a wave-absorbing performance chart of examples 1, 2, 3, 4 and comparative examples.
Wherein the reference numerals in fig. 3 are as follows: a-example 1, b-example 2, c-example 3, d-example 4, e-comparative example.
Detailed Description
The embodiments of the present invention are described below with reference to specific embodiments, and other advantages and effects of the present invention will be readily apparent to those skilled in the art from the disclosure of the present invention.
Before the present embodiments are further described, it is to be understood that the scope of the invention is not limited to the particular embodiments described below; it is also to be understood that the terminology used in the examples is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention. Test methods in which specific conditions are not specified in the following examples are generally carried out under conventional conditions or under conditions recommended by the respective manufacturers.
When numerical ranges are given in the examples, it is understood that both endpoints of each of the numerical ranges and any value therebetween can be selected unless the invention otherwise indicated. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In addition to the specific methods, devices, and materials used in the examples, any methods, devices, and materials similar or equivalent to those described in the examples may be used in the practice of the invention in addition to the specific methods, devices, and materials used in the examples, in keeping with the knowledge of one skilled in the art and with the description of the invention.
In the examples of the present application, the products obtained by the preparation of each example and comparative example were irradiated with an irradiation source
Figure BDA0003066827470000041
To determine the crystal structure.
In the embodiment of the application, the tin source adopted in each embodiment is tin tetrachloride pentahydrate, and the nickel source is nickel chloride hexahydrate; the mass ratio of the tin tetrachloride pentahydrate, the nickel chloride hexahydrate, the thioacetamide and the ethanol is determined according to the optimum ratio determined by research, namely the mass ratio of the tin tetrachloride pentahydrate, the nickel chloride hexahydrate, the thioacetamide and the ethanol is 3.16: 2.14: 2.7: 233.05.
in the examples of the present application, the morphology of the products obtained by the respective examples and comparative examples was observed by using a scanning electron microscope and a transmission electron microscope.
In the examples of the present application, the products obtained in the preparation of each example and comparative example were uniformly dispersed in paraffin wax, which was 15% by weight of the total weight, and then pressed by a die into coaxial sample rings having an outer diameter of 7.0mm and an inner diameter of 3.04 mm. The electrical complex permittivity and complex permeability of the material are measured by adopting a Ceyear 3672B-S vector network analyzer based on the measurement technical requirement of a coaxial line transmission/reflection method in the American society for testing and materials standard ASTM D7449/D7449M-08, and the RL value of the material is calculated according to the transmission line theory.
Example 1
In this embodiment, the preparation of the popcorn-based carbon-based composite material includes the steps of:
(1) ultrasonically cleaning pure popcorn with deionized water and absolute ethyl alcohol for 3 times, each time for 10 minutes, placing in an oven at 60 ℃, and drying for 24 hours; and calcining the dried popcorn in an argon atmosphere at 600 ℃ for 120min, wherein the temperature rise rate of the calcination is 5 ℃/min, and then cooling to room temperature to obtain the carbonized popcorn.
(2) 0.631g of tin tetrachloride pentahydrate, 0.428g of nickel chloride hexahydrate and 0.54g of thioacetamide were dissolved in 59ml of anhydrous ethanol, stirred for 10min, then 1ml of deionized water was added, and stirred for 10min to form a uniform mixture.
(3) Adding 10mg of carbonized popcorn into the mixture, continuously stirring for 6h, pouring into a stainless steel autoclave with a polytetrafluoroethylene lining, heating to 160 ℃ in a microwave-assisted heating manner for reaction, preserving the temperature for 8h, and then cooling to room temperature to obtain a reaction product.
(4) And (3) filtering and washing the reaction product respectively by using deionized water and absolute ethyl alcohol for 3 times, putting the reaction product into an oven at the temperature of 60 ℃, and drying the reaction product for 24 hours to obtain the carbon-based composite material based on the popcorn.
As can be seen from the XRD pattern of FIG. 1, this example contains typical amorphous carbon diffraction peaks, and the carbon-based composite material is composed of carbon and NiS2And SnS2Three substances.
As can be seen from the graph d in the SEM image of FIG. 2, the carbon-based composite material has a porous structure, and after carbonization at 600 ℃, the obtained carbon-based pores are relatively uniform, and the pore diameter is between 50 μm and 100 μm.
As can be seen from the wave-absorbing property diagrams of Table 1 and FIG. 3, the carbon-based composite material of example 1 has a thickness ranging from 1.0 mm to 5.0mm, and has a minimum Reflection Loss (RL) of PC6-NSS when the frequency is 7.56GHz and the thickness is 5mmmin) Is-16.2 dB; when the thickness of the carbon-based composite material is 4.5mm, the maximum effective absorption bandwidth is 2.8GHz, which indicates that the carbon-based composite material prepared in the embodiment has general wave-absorbing performance.
Example 2
In this example, the preparation of the popcorn-based carbon-based composite material includes the following steps:
(1) ultrasonically cleaning pure popcorn with deionized water and absolute ethyl alcohol for 3 times, each time for 10 minutes, placing in an oven at 60 ℃, and drying for 24 hours; and calcining the dried popcorn at 700 ℃ for 120min in an argon atmosphere at a heating rate of 5 ℃/min, and then cooling to room temperature to obtain carbonized popcorn.
(2) 0.631g of tin tetrachloride pentahydrate, 0.428g of nickel chloride hexahydrate and 0.54g of thioacetamide were dissolved in 59ml of anhydrous ethanol, stirred for 10min, then 1ml of deionized water was added, and stirred for 10min to form a uniform mixture.
(3) Adding 10mg of carbonized popcorn into the mixture, continuously stirring for 6h, pouring into a stainless steel autoclave with a polytetrafluoroethylene lining, heating to 160 ℃ in a microwave-assisted heating manner for reaction, preserving the heat for 8h, and then cooling to room temperature to obtain a reaction product.
(4) And (3) filtering and washing the reaction product respectively by using deionized water and absolute ethyl alcohol for 3 times, placing the reaction product in an oven at the temperature of 60 ℃, and drying the reaction product for 24 hours to obtain the carbon-based composite material based on the popcorn.
As can be seen from the XRD pattern of FIG. 1, this example contains typical amorphous carbon diffraction peaks, indicating that the carbon-based composite material is composed of carbon and NiS2And SnS2Three substances.
As can be seen from the graph e in the SEM image of fig. 2, the carbon-based composite material has a porous structure, and after carbonization at 700 ℃, partial pores are reduced in shrinkage, thereby causing some larger pores to appear, and the pore size is not uniform beyond 100 μm.
As can be seen from the wave-absorbing performance graphs of Table 1 and FIG. 3, the thickness range of the carbon-based composite material obtained in example 2 is 1.0-5.0mm, and when the frequency is 7.56GHz and the thickness is 3mm, the minimum reflection loss RL of the carbon-based composite material is obtainedminIs-20.9 dB; when the thickness of the carbon-based composite material is 1.5mm, the maximum effective absorption bandwidth is 2.4GHz, which indicates that the carbon-based composite material obtained in the embodiment has general wave-absorbing performance.
Example 3
In this example, the preparation of the popcorn-based carbon-based composite material includes the following steps:
(1) ultrasonically cleaning pure popcorn with deionized water and absolute ethyl alcohol for 3 times, each time for 10 minutes, placing in a drying oven at 60 ℃, and drying for 24 hours; and calcining the dried popcorn in an argon atmosphere at 800 ℃ for 120min, wherein the temperature rise rate of the calcination is 5 ℃/min, and then cooling to room temperature to obtain the carbonized popcorn.
(2) 0.631g of tin tetrachloride pentahydrate, 0.428g of nickel chloride hexahydrate and 0.54g of thioacetamide were dissolved in 59ml of anhydrous ethanol, stirred for 10min, then 1ml of deionized water was added, and stirred for 10min to form a uniform mixture.
(3) Adding 10mg of carbonized popcorn into the mixture, continuously stirring for 6h, pouring into a stainless steel autoclave with a polytetrafluoroethylene lining, heating to 160 ℃ in a microwave-assisted heating manner for reaction, preserving the temperature for 8h, and then cooling to room temperature to obtain a reaction product.
(4) And (3) filtering and washing the reaction product respectively by using deionized water and absolute ethyl alcohol for 3 times, placing the reaction product in an oven at the temperature of 60 ℃, and drying the reaction product for 24 hours to obtain the carbon-based nano composite material based on the popcorn.
As can be seen from the XRD pattern in figure 1, the composite material contains typical amorphous carbon diffraction peaks and is made of carbon and NiS2And SnS2Three substances.
As can be seen from the SEM images of a and b and the TEM image of a C in FIG. 2, the carbon-based composite material has a porous structure, gradually uneven pore distribution and increased macropores, and can reach 150 μm.
As can be seen from the wave-absorbing property diagrams of Table 1 and FIG. 3, the thickness range of the carbon-based composite material obtained in example 3 is 1.0-5.0mm, and when the frequency is 14.92GHz and the thickness is 1.57mm, the minimum reflection loss RL of the carbon-based composite material isminIs-53.0 dB, and the absorption bandwidth is 48 GHz; minimum reflection loss RL when the thickness of the carbon-based composite material is 2.11mmminAnd is-46.3 dB, which shows that the carbon-based composite material obtained by the embodiment has excellent wave-absorbing performance.
Example 4
In this example, the preparation of the popcorn-based carbon-based composite material includes the following steps:
(1) ultrasonically cleaning pure popcorn with deionized water and absolute ethyl alcohol for 3 times, each time for 10 minutes, placing in an oven at 60 ℃, and drying for 24 hours; and calcining the dried popcorn in an argon atmosphere at 900 ℃ for 120min, wherein the temperature rise rate of the calcination is 5 ℃/min, and then cooling to room temperature to obtain the carbonized popcorn.
(2) 0.631g of tin tetrachloride pentahydrate, 0.428g of nickel chloride hexahydrate and 0.54g of thioacetamide were dissolved in 59ml of anhydrous ethanol, stirred for 10min, then 1ml of deionized water was added, and stirred for 10min to form a uniform mixture.
(3) Adding 10mg of carbonized popcorn into the mixture, continuously stirring for 6h, pouring into a stainless steel autoclave with a polytetrafluoroethylene lining, heating to 160 ℃ in a microwave-assisted heating manner for reaction, preserving the temperature for 8h, and then cooling to room temperature to obtain a reaction product.
(4) And (3) filtering and washing the reaction product respectively by using deionized water and absolute ethyl alcohol for 3 times, putting the reaction product into an oven at the temperature of 60 ℃, and drying the reaction product for 24 hours to obtain the carbon-based nano composite material based on the popcorn.
As can be seen from the XRD pattern of FIG. 1, this example contains typical amorphous carbon diffraction peaks, and the carbon-based composite material is composed of carbon and NiS2And SnS2Three substances.
As can be seen from the SEM image of fig. f in fig. 2, the carbon-based composite material has a porous structure, more uneven pore distribution, more macropores, and a pore diameter close to 200 μm.
As can be seen from the wave-absorbing performance graphs of Table 1 and FIG. 3, the thickness range of the carbon-based carbon composite material obtained in example 4 is 1.0-5.0mm, and when the frequency is 14.92GHz and the thickness is 1.4mm, the minimum reflection loss RL of the carbon-based carbon composite material isminIs-32.5 dB, and the absorption bandwidth is 4.3GHz, which shows that the carbon-based composite material obtained in the embodiment has general wave-absorbing performance.
Comparative examples
In this comparative example, carbonized popcorn was prepared, comprising the steps of:
ultrasonically cleaning pure popcorn with deionized water and absolute ethyl alcohol for 3 times, each time for 10 minutes, placing in an oven at 60 ℃, and drying for 24 hours; and calcining the dried popcorn in an argon atmosphere at 800 ℃ for 120min, wherein the temperature rise rate of the calcination is 5 ℃/min, and then cooling to room temperature to obtain the carbonized popcorn.
As can be seen from the XRD pattern of fig. 1, this comparative example contains typical amorphous carbon diffraction peaks.
As can be seen from the wave-absorbing property graphs in Table 1, the carbonized popcorn prepared in this comparative example has a thickness ranging from 1.0 to 5.0mm, and a minimum reflection loss RL of the carbonized popcorn at a frequency of 18GHz and a thickness of 1mmminIs-10.9 dB; when the thickness of the carbonized popcorn is 1mm, the maximum effective absorption bandwidth is 0.6GHz, which shows that the carbonized popcorn obtained by the comparative example has poor wave-absorbing performance.
TABLE 1
Figure BDA0003066827470000081
As can be seen from Table 1, the composite material of example 3 shows excellent wave-absorbing performance at a light filling ratio (25 wt%), a thin thickness (1.57mm) and a wide frequency range (12.0-16.8GHz), and has great application potential.
The foregoing embodiments are merely illustrative of the principles and utilities of the present invention and are not intended to limit the invention. Those skilled in the art can modify or change the above-described embodiments without departing from the spirit and scope of the present invention. Accordingly, it is intended that all equivalent modifications or changes which can be made by those skilled in the art without departing from the spirit and technical spirit of the present invention be covered by the claims of the present invention.

Claims (9)

1. A carbon-based composite material based on popcorn is characterized in that the material is a carbon-based material with a NiS surface covered by NiS2/SnS2Nanosheets; the carbon base is porous, and the average pore diameter is 50-200 mu m; the material consists of carbon, nickel sulfide and tin sulfide, wherein the molar ratio of the carbon to the nickel to the tin to the sulfur is (10-30): (0.5-2.2): 1: (1-6).
2. A process of preparing popcorn based carbon based nanocomposite according to claim 1, comprising the steps of: carrying out hydrothermal reaction on a mixture of a nickel source, a tin source and a sulfur source and carbonized popcorn to obtain the popcorn-based carbon-based composite material; the preparation method of the carbonized popcorn comprises the following steps: calcining the popcorn at 500-900 ℃ under a protective atmosphere to obtain the carbonized popcorn; the nickel source is nickel chloride, the tin source is tin chloride, and the sulfur source is thioacetamide.
3. The method according to claim 2, wherein the carbonized popcorn has a specific surface area of 2m2/g～30m2The pore diameter is 30-180 mu m.
4. The preparation method according to claim 2, wherein the temperature rise rate of the calcination is 2 to 10 ℃/min;
and/or the calcining time is 80-200 min;
and/or the protective atmosphere is selected from one or more of nitrogen and argon.
5. The method according to claim 2, wherein the mixture is obtained by dissolving a nickel source, a sulfur source, and a sulfur source in ethanol.
6. The preparation method according to claim 2, wherein the mass ratio of the tin chloride to the nickel chloride to the thioacetamide to the ethanol is 1: (0.2-1.0): (0.2-1.6): (50-140).
7. The preparation method according to claim 2, wherein the mass ratio of the carbonized popcorn and the tin source is 1 (2-10).
8. The method according to claim 2, wherein the temperature of the hydrothermal reaction is 100 ℃ to 200 ℃.
9. Use of a popcorn-based carbon-based composite material according to claim 1 as a wave-absorbing material in the field of electromagnetic waves.
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